Canonical Allele Identifier: CA2690769931

Gene: FBP1

Linked Data

• gnomAD v4: 9-94639306-GCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94639307_94639308del , CM000671.2:g.94639307_94639308del	GRCh38
NC_000009.11:g.97401589_97401590del , CM000671.1:g.97401589_97401590del	GRCh37
NC_000009.10:g.96441410_96441411del	NCBI36
NG_008174.1:g.5942_5943del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682520.1:c.3_4del	ENSP00000507547.1:p.Met1IlefsTer2
ENST00000375326.9:c.3_4del MANE Select	ENSP00000364475.5:p.Met1IlefsTer2
ENST00000375326.8:c.3_4del	ENSP00000364475.4:p.Met1IlefsTer2
ENST00000414122.1:c.-83+736_-83+737del	ENSP00000411619.1:n.-83+736_-83+737del
ENST00000415431.5:c.3_4del	ENSP00000408025.1:p.Met1IlefsTer2
NM_000507.3:c.3_4del	NP_000498.2:p.Met1IlefsTer2
NM_001127628.1:c.3_4del	NP_001121100.1:p.Met1IlefsTer2
XM_006717005.2:c.-77+736_-77+737del	XP_006717068.1:n.-77+736_-77+737del
XM_006717005.4:c.-77+736_-77+737del	XP_006717068.1:n.-77+736_-77+737del
NM_000507.4:c.3_4del MANE Select	NP_000498.2:p.Met1IlefsTer2
NM_001127628.2:c.3_4del	NP_001121100.1:p.Met1IlefsTer2